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The sliding averages of 61 points (12.5 min interval) of calculated Poynting fluxes are used to examine changes in energy flow associated with Pc 5 signals.
Constant reactor temperature of 25 ± 2 °C was maintained by running the bath in the cyclic operation mode of 'on' and 'off.' Samples were withdrawn at 10 min interval of time and quenched immediately in an ice bath to stop the rate of decolorization of BG dye.
The results are displayed as sum of the average fluorescence intensities of 495 to 505 nm in the saturation phase (24 h to 48 h in 30 min interval) of the curve.
In CA1 pyramidal cells from unstimulated control slices we found a broad distribution of mIPSC amplitudes with a median quantal amplitude of 15.7±0.8 pA at −70 mV (n = 7; based on 1890±291 events/cell within the 10 min interval of evaluation).
Strikingly, in a 120 min interval of observation, the GA of control cells appeared unperturbed and rather static.
Following 15 min interval of supine rest, measurements of arterial stiffness (see measurements) and BP were obtained and a baseline blood sample was collected.
Similar(53)
Analysis of 10 min intervals of the sample of 12 units with spontaneous activity revealed the same differences (Fig. 2a).
Each session consisted of five, 3 min intervals of walking, jogging or cycling at 65-95% maximal heart rate (MHR) with 3 min of low-intensity exercise (<65% MHR) between intervals.
The degradation of the dye was monitored by measuring the absorption maximum of methylene blue at 661 nm at 30 min intervals of reaction.
The amount of release of curcuminoids was determined at 15 min intervals, followed by 30 min intervals of monitoring the variation of absorbance in the UV Vis absorption spectroscopy, with the peak at 427 nm (λmax of curcuminoids).
Forty-five minute timelapse (5 min intervals) of a cell that has assembled a replisome (Ssb) at oriC.
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